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FDA 510(k)

BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES

K-Number: K911606 · 1991-07-09

Decision Date1991-07-09
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1991-07-09 under 510(k) number K911606. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES?

BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES is a medical device that received FDA 510(k) clearance on 1991-07-09. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K911606.

When did BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES receive FDA 510(k) clearance?

BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES received FDA 510(k) clearance on 1991-07-09, under 510(k) number K911606.

Who is the listed applicant for BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES?

The FDA product code for BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES is KDD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Baxter Healthcare Corp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 504 devices →

Related Devices (Code: KDD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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